Dual clinical features of fine and rough scales seen in a combined ichthyosis vulgaris and X-linked recessive ichthyosis patient with atopic dermatitis
Yoshimasa Nakane
Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Search for more papers by this authorTakenori Yoshikawa
Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Search for more papers by this authorCorresponding Author
Takuya Takeichi
Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Correspondence
Takuya Takeichi and Masashi Akiyama, Department of Dermatology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Email: [email protected] and [email protected]
Search for more papers by this authorMichihiro Kono
Department of Dermatology and Plastic Surgery, Akita University Graduate School of Medicine, Akita, Japan
Search for more papers by this authorCorresponding Author
Masashi Akiyama
Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Correspondence
Takuya Takeichi and Masashi Akiyama, Department of Dermatology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Email: [email protected] and [email protected]
Search for more papers by this authorYoshimasa Nakane
Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Search for more papers by this authorTakenori Yoshikawa
Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Search for more papers by this authorCorresponding Author
Takuya Takeichi
Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Correspondence
Takuya Takeichi and Masashi Akiyama, Department of Dermatology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Email: [email protected] and [email protected]
Search for more papers by this authorMichihiro Kono
Department of Dermatology and Plastic Surgery, Akita University Graduate School of Medicine, Akita, Japan
Search for more papers by this authorCorresponding Author
Masashi Akiyama
Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Correspondence
Takuya Takeichi and Masashi Akiyama, Department of Dermatology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Email: [email protected] and [email protected]
Search for more papers by this author
REFERENCES
- 1Nomura T, Sandilands A, Akiyama M, Liao H, Evans AT, Sakai K, et al. Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis. J Allergy Clin Immunol. 2007; 119: 434–440.
- 2Hand JL, Runke CK, Hodge JC. The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray. J Am Acad Dermatol. 2015; 72: 617–627.
- 3Süßmuth K, Gruber R, Rodriguez E, Traupe H, Amler S, Sánchez-Guijo A, et al. Increased prevalence of filaggrin deficiency in 51 patients with recessive X-linked ichthyosis presenting for dermatological examination. J Invest Dermatol. 2018; 138: 709–711.
- 4Ramesh R, Chen H, Kukula A, Wakeling EL, Rustin MH, McLean WH. Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations. J Dermatol Sci. 2011; 64: 159–162.
- 5Zhang Q, Si N, Liu Y, Zhang D, Wang R, Zhang Y, et al. Steroid sulfatase and filaggrin mutations in a boy with severe ichthyosis, elevated serum IgE level and moyamoya syndrome. Gene. 2017; 628: 103–108.
